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Stanley C Xie

Showing results (11-20 of 23) with videos related to

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ACS Infectious Diseases|May 28, 2021
High Throughput Screening to Identify Selective and Nonpeptidomimetic Proteasome Inhibitors As AntimalarialsLydia Mata-Cantero, Stanley C Xie, Mercedes García, et al.
Nature Communications|September 20, 2018
Artemisinin kills malaria parasites by damaging proteins and inhibiting the proteasomeJessica L Bridgford, Stanley C Xie, Simon A Cobbold, et al.
Cell Reports|November 28, 2019
Decreased K13 Abundance Reduces Hemoglobin Catabolism and Proteotoxic Stress, Underpinning Artemisinin ResistanceTuo Yang, Lee M Yeoh, Madel V Tutor, et al.
Plos Biology|April 23, 2015
Targeting the cell stress response of Plasmodium falciparum to overcome artemisinin resistanceCon Dogovski, Stanley C Xie, Gaetan Burgio, et al.
Nature Microbiology|August 7, 2019
The structure of the PA28-20S proteasome complex from Plasmodium falciparum and implications for proteostasisStanley C Xie, Riley D Metcalfe, Eric Hanssen, et al.
Plos Pathogens|July 8, 2025
Natural product-mediated reaction hijacking mechanism validates Plasmodium aspartyl-tRNA synthetase as an antimalarial drug targetNutpakal Ketprasit, Chia-Wei Tai, Vivek Kumar Sharma, et al.
Journal of Medicinal Chemistry|October 31, 2018
Target Validation and Identification of Novel Boronate Inhibitors of the Plasmodium falciparum ProteasomeStanley C Xie, David L Gillett, Natalie J Spillman, et al.
Biorxiv : the Preprint Server for Biology|May 25, 2026
Potent reaction hijacking inhibitors of <i>Plasmodium falciparum</i> asparagine tRNA synthetaseXi Ye, Lisl Y Esherick, Nutpakal Ketprasit, et al.
Science (New York, N.Y.)|June 2, 2022
Reaction hijacking of tyrosine tRNA synthetase as a new whole-of-life-cycle antimalarial strategyStanley C Xie, Riley D Metcalfe, Elyse Dunn, et al.
Plos Pathogens|December 9, 2024
A potent and selective reaction hijacking inhibitor of Plasmodium falciparum tyrosine tRNA synthetase exhibits single dose oral efficacy in vivoStanley C Xie, Chia-Wei Tai, Craig J Morton, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
ACS Infectious Diseases|May 28, 2021
High Throughput Screening to Identify Selective and Nonpeptidomimetic Proteasome Inhibitors As AntimalarialsLydia Mata-Cantero, Stanley C Xie, Mercedes García, et al.
Nature Communications|September 20, 2018
Artemisinin kills malaria parasites by damaging proteins and inhibiting the proteasomeJessica L Bridgford, Stanley C Xie, Simon A Cobbold, et al.
Cell Reports|November 28, 2019
Decreased K13 Abundance Reduces Hemoglobin Catabolism and Proteotoxic Stress, Underpinning Artemisinin ResistanceTuo Yang, Lee M Yeoh, Madel V Tutor, et al.
Plos Biology|April 23, 2015
Targeting the cell stress response of Plasmodium falciparum to overcome artemisinin resistanceCon Dogovski, Stanley C Xie, Gaetan Burgio, et al.
Nature Microbiology|August 7, 2019
The structure of the PA28-20S proteasome complex from Plasmodium falciparum and implications for proteostasisStanley C Xie, Riley D Metcalfe, Eric Hanssen, et al.
Plos Pathogens|July 8, 2025
Natural product-mediated reaction hijacking mechanism validates Plasmodium aspartyl-tRNA synthetase as an antimalarial drug targetNutpakal Ketprasit, Chia-Wei Tai, Vivek Kumar Sharma, et al.
Journal of Medicinal Chemistry|October 31, 2018
Target Validation and Identification of Novel Boronate Inhibitors of the Plasmodium falciparum ProteasomeStanley C Xie, David L Gillett, Natalie J Spillman, et al.
Biorxiv : the Preprint Server for Biology|May 25, 2026
Potent reaction hijacking inhibitors of <i>Plasmodium falciparum</i> asparagine tRNA synthetaseXi Ye, Lisl Y Esherick, Nutpakal Ketprasit, et al.
Science (New York, N.Y.)|June 2, 2022
Reaction hijacking of tyrosine tRNA synthetase as a new whole-of-life-cycle antimalarial strategyStanley C Xie, Riley D Metcalfe, Elyse Dunn, et al.
Plos Pathogens|December 9, 2024
A potent and selective reaction hijacking inhibitor of Plasmodium falciparum tyrosine tRNA synthetase exhibits single dose oral efficacy in vivoStanley C Xie, Chia-Wei Tai, Craig J Morton, et al.
Pageof 3